Canonical Allele Identifier: PA2825224546
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087171
ClinVar RCV Id: RCV002999960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Ala103Thr
CA344206396
NM_001001432.3:c.307G>A